Technical Field
[0001] The present invention relates to a spectacle lens having a hard coat layer.
Background Art
[0002] Although spectacle lenses are required to have various properties, a nature to be
hardly scratched as a user uses the spectacle lens in daily life, namely, abrasion
resistance is required. Although a spectacle lens is required to exhibit various properties,
a nature to be hardly scratched by the use in daily life by the user of the spectacle,
namely, abrasion resistance is required. A hard coat layer is almost formed on spectacle
lenses, particularly plastic spectacle lenses for the purpose of preventing scratches.
Usually, the hard coat is deposited in a film thickness range of from 1 to 3 µm to
impart abrasion resistance to the spectacle lens inusual use. In Patent Literature
1, a spectacle lens including hard coat having a thicker film thickness than the hard
coat in the prior art is disclosed for the purpose of further suppressing the occurrence
of interference fringes.
Citation List
Patent Literature
Summary of Invention
Technical Problem
[0004] According to the optical article described in Patent Literature 1, although it is
possible to suppress the interference fringe and further to improve the abrasion resistance
which has been hitherto said by using a functional layer including a hard coat layer,
there is a problem that it is difficult to achieve adhesion between the hard coat
layer and the antireflection film because of an increase in film thickness.
[0005] Accordingly, an object of the present invention is to provide a spectacle lens in
which excellent adhesive property is exhibited between a hard coat layer and a functional
layer such as an antireflection layer formed on the hard coat layer.
Solution to Problem
[0006] The present invention relates to the following spectacle lens.
- [1] A spectacle lens including a lens substrate, a hard coat layer, and an antireflection
layer, in which the hard coat layer has a film thickness of 10 µm or more and 50 µm
or less and the hard coat layer is obtained by curing a curable composition containing
inorganic oxide particles, a silane coupling agent, and a polyfunctional epoxy compound
contained at 20% by mass or more and 40% by mass or less in a matrix component.
- [2] The spectacle lens according to [1], in which the inorganic oxide particles are
silica particles.
- [3] The spectacle lens according to [1] or [2], in which the silane coupling agent
has an organic group bonded to a silicon atom and an alkoxy group bonded to a silicon
atom.
- [4] The spectacle lens according to any one of [1] to [3], in which the polyfunctional
epoxy compound has two or three epoxy groups.
- [5] The spectacle lens according to any one of [1] to [4], further including an interference
fringe suppressing layer between the lens substrate and the hard coat layer.
Advantageous Effects of Invention
[0007] According to the present invention, it is possible to provide a spectacle lens in
which excellent adhesive property is exhibited between a hard coat layer and a functional
layer such as an antireflection layer formed on the hard coat layer.
Description of Embodiments
[0008] The spectacle lens of the present invention is a spectacle lens which includes a
lens substrate, a hard coat layer, and an antireflection layer and in which the hard
coat layer has a film thickness of 10 µm or more and 50 µm or less and the hard coat
layer is obtained by curing a curable composition containing inorganic oxide particles,
a silane coupling agent, and a polyfunctional epoxy compound contained 20% by mass
or more and 40% by mass or less in a matrix component.
[0009] Excellent adhesive property is exhibited between a hard coat layer and a functional
layer such as an antireflection layer formed on the hard coat layer as a polyfunctional
epoxy compound is contained in the curable composition to be used in the formation
of the hard coat layer in the above range.
[0010] A spectacle lens having a high film peeling off load value is obtained as the film
thickness of the hard coat layer is 10 µm or more and 50 µm or less. In addition,
the film thickness of the hard coat layer is preferably 15 µm or more and more preferably
18 µm or more from the viewpoint of obtaining a spectacle lens having a high film
peeling off load value. The film thickness is preferably 40 µm or less and more preferably
30 µm or less from the viewpoint of suppressing the generation of initial cracks.
The "film thickness" means an average film thickness, and the measuring method thereof
is described in Examples.
[0011] The content of the polyfunctional epoxy compound in the curable composition to be
used in the formation of the hard coat layer is 20% by mass or more and more preferably
25% by mass or more in the matrix component from the viewpoint of high adhesive property
between the hard coat layer and a functional layer such as an antireflection layer
formed on the hard coat layer. The content of the polyfunctional epoxy compound is
40% by mass or less in the matrix component. In the present specification, the matrix
component means a silane coupling agent and a polyfunctional epoxy compound.
[0012] A hard coat layer exhibiting excellent adhesive property is obtained as the polyfunctional
epoxy compound is added thereto.
[0013] Hereinafter, the configuration of the spectacle lens of the present invention will
be described in detail.
(Lens substrate)
[0014] Examples of the material to be used in the lens substrate of a spectacle lens may
include plastics such as a polyurethane-based material (for example, polyurethane,
polyurethane urea, polythiourethane), polycarbonate, and diethylene glycol-bis-allyl-carbonate
and inorganic glass. The thickness and diameter of the lens substrate are not particularly
limited. Usually, the thickness is about from 1 to 30 mm and the diameter is about
from 50 to 100 mm. In a case in which the spectacle lens of the present invention
is a spectacle lens for vision correction, it is usual to use those having a refractive
index ne of about from 1. 5 to 1. 8 as the lens substrate. Colorless ones are usually
used as the lens substrate, but it is also possible to use colored ones as long as
the transparency is not impaired. In addition, the surface shape of the substrate
on which a cured film is formed is not particularly limited, and it can be an arbitrary
shape such as a flat shape, a convex shape, or a concave shape.
[Functional layer]
[0015] In the spectacle lens of the present invention, the lens substrate is provided with
at least the hard coat layer and the antireflection layer. Examples of other functional
layers may include a primer layer, an interference fringe suppressing layer, a polarizing
layer, and a photochromic layer. In addition, it is also possible to further provide
functional layers such as an antiref lection layer, a water repellent film, an ultraviolet
absorbing film, an infrared absorbing film, a photochromic film, and an antistatic
film on the hard coat layer if necessary. With regard to functional layers other than
these, known techniques related to spectacle lenses can be applied.
[0016] The hard coat layer may be directly formed on the lens substrate surface, or it may
be indirectly formed thereon via one or more other functional layers.
[0017] The spectacle lens of the present invention preferably includes a lens substrate,
a hard coat layer provided on the lens substrate, and an antiref lection layer provided
on the hard coat layer, it preferably includes a lens substrate, a primer layer provided
on the lens substrate, a hard coat layer provided on the primer layer, and an antireflection
layer provided on the hard coat layer, and it more preferably includes a lens substrate,
an interference fringe suppressing layer provided on the lens substrate, a primer
layer provided on the interference fringe suppressing layer, a hard coat layer provided
on the primer layer, and an antireflection layer provided on the hard coat layer.
(Hard coat layer)
[0018] The hard coat layer is obtained, for example, by curing a curable composition containing
inorganic oxide particles (hereinafter, referred to as the "component (A)"), a silane
coupling agent (hereinafter, referredtoasthe "component (B) "), and a polyfunctional
epoxy compound (hereinafter, referred to as the "component (C)").
[0019] Examples of the component (A) may include particles of tungsten oxide (WO
3), zinc oxide (ZnO), silicon oxide (SiO
2), aluminum oxide (Al
2O
3), titanium oxide (TiO
2), zirconium oxide (ZrO
2), tin oxide (SnO
2), beryllium oxide (BeO), antimony oxide (Sb
2O
5), and the like, and the component (A) is preferably silicon oxide. These metal oxide
particles may be used singly or two or more kinds thereof may be concurrently used.
In addition, it is also possible to use composite oxide particles of two or more kinds
of inorganic oxides. The particle size of the inorganic oxide particles is preferably
in a range of from 5 to 3 0 nm from the viewpoint of achieving both abrasion resistance
and optical properties. Among these inorganic oxide particles, silica particles are
preferable from the viewpoint of obtaining excellent adhesive property with a functional
layer such as an antireflection layer.
[0020] The component (B) is a silane coupling agent, and it is preferably a silane coupling
agent having an organic group to be bonded to a silicon atom and a hydrolyzable group.
[0021] Examples of the hydrolyzable group may include an alkoxy group, an aryloxy group,
and a hydroxyl group, and the hydrolyzable group is preferably an alkoxy group.
[0022] The silane coupling agent is preferably an organic silicon compound represented by
the following general formula (I) or a hydrolysate thereof.
(R
1)
a(R
3)
bSi(OR
2)
4-(a+b) ... (I)
[0023] In the general formula (I), a is 1 and b is 0 or 1.
[0024] R
1 represents an organic group having a functional group such as an epoxy group such
as a glycidoxy group, a vinyl group, a methacryloxy group, an acryloxy group, a mercapto
group, an amino group, or a phenyl group, and preferably R
1 represents an organic group having an epoxy group. The functional group may be directly
bonded to a silicon atom or indirectly bonded thereto via a linking group such as
an alkylene group.
[0025] R
2 represents, for example, ahydrogenatom, an alkyl group, an acyl group, or an aryl
group, and preferably R
2 represents an alkyl group.
[0026] The alkyl group represented by R
2 is, for example, a straight-chain or branched alkyl group having from 1 to 4 carbon
atoms, and specific examples thereof may include a methyl group, an ethyl group, a
propyl group, and a butyl group, and preferably the alkyl group is a methyl group
or an ethyl group.
[0027] The acyl group represented by R
2 is, for example, an acyl group having from 1 to 4 carbon atoms, and specific examples
thereof may include an acetyl group, a propionyl group, an oleyl group, and a benzoyl
group.
[0028] The aryl group represented by R
2 is, for example, an aryl group having from 6 to 10 carbon atoms, and specific examples
thereof may include a phenyl group, a xylyl group, and a tolyl group.
[0029] R
3 can be an alkyl group or an aryl group.
[0030] The alkyl group represented by R
3 is, for example, a straight-chain or branched alkyl group having from 1 to 6 carbon
atoms, and specific examples thereof may include a methyl group, an ethyl group, a
propyl group, a butyl group, a pentyl group, and a hexyl group.
[0031] The aryl group represented by R
3 is, for example, an aryl group having from 6 to 10 carbon atoms, and specific examples
thereof may include a phenyl group, a xylyl group, and a tolyl group.
[0032] Specific examples of the component (B) may include glycidoxymethyltrimethoxysilane,
glycidoxymethyltriethoxysilane, α-glycidoxyethyltriethoxysilane, β-glycidoxyethyltrimethoxysilane,
β-glycidoxyethyltriethoxysilane, α-glycidoxypropyltrimethoxysilane, α-glycidoxypropyltriethoxysilane,
β-glycidoxypropyltrimethoxysilane, β-glycidoxypropyltriethoxysilane, γ-glycidoxypropyltrimethoxysilane,
γ-glycidoxypropyltriethoxysilane, γ-glycidoxypropyltripropoxysilane, γ-glycidoxypropyltributoxysilane,
γ-glycidoxypropyltriphenoxysilane, α-glycidoxybutyltrimethoxysilane, α-glycidoxybutyltriethoxysilane,
β-glycidoxybutyltrimethoxysilane, β-glycidoxybutyltriethoxysilane, γ-glycidoxybutyltrimethoxysilane,
γ-glycidoxybutyltriethoxysilane, δ-glycidoxybutyltrimethoxysilane, δ-glycidoxybutyltriethoxysilane,
(3,4-epoxycyclohexyl)methyltrimethoxysilane, (3,4-epoxycyclohexyl)methyltriethoxysilane,
β-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, β-(3,4-epoxycyclohexyl)ethyltriethoxysilane,
β-(3,4-epoxycyclohexyl)ethyltripropoxysilane, β-(3,4-epoxycyclohexyl)ethyltributoxysilane,
β-(3,4-epoxycyclohexyl)ethyltriphenoxysilane, γ-(3,4-epoxycyclohexyl)propyltrimethoxysilane,
γ-(3,4-epoxycyclohexyl)propyltriethoxysilane, δ-(3,4-epoxycyclohexyl)butyltrimethoxysilane,
δ-(3,4-epoxycyclohexyl)butyltriethoxysilane, glycidoxymethylmethyldimethoxysilane,
glycidoxymethylmethyldiethoxysilane, α-glycidoxyethylmethyldimethoxysilane, α-glycidoxyethylmethyldiethoxysilane,
β-glycidoxyethylmethyldimethoxysilane, β-glycidoxyethylmethyldiethoxysilane, α-glycidoxypropylmethyldimethoxysilane,
α-glycidoxypropylmethyldiethoxysilane, β-glycidoxypropylmethyldimethoxysilane, β-glycidoxypropylmethyldiethoxysilane,
γ-glycidoxypropylmethyldimethoxysilane, γ-glycidoxypropylmethyldiethoxysilane, γ-glycidoxypropylmethyldipropoxysilane,
γ-glycidoxypropylmethyldibutoxysilane, γ-glycidoxypropylmethyldiphenoxysilane, γ-glycidoxypropylethyldimethoxysilane,
γ-glycidoxypropylethyldiethoxysilane, γ-lycidoxypropylvinyldimethoxysilane, γ-glycidoxypropylvinyldiethoxysilane,
γ-glycidoxypropylphenyldimethoxysilane, γ-glycidoxypropylphenyldiethoxysilane,
vinyltrimethoxysilane, vinyltriacetoxysilane, vinyltrimethoxyethoxysilane, phenyltrimethoxysilane,
phenyltriethoxysilane, phenyltriacetoxysilane, γ-chloropropyltrimethoxysilane, γ-chloropropyltriethoxysilane,
γ-chloropropyltriacetoxysilane, 3,3,3-trifluoropropyltrimethoxysilane, γ-methacryloxypropyltrimethoxysilane,
γ-mercaptopropyltrimethoxysilane, γ-mercaptopropyltriethoxysilane, β-cyanoethyltriethoxysilane,
chloromethyltrimethoxysilane, chloromethyltriethoxysilane, N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane,
N-(β-aminoethyl)-γ-aminopropylmethyldimethoxysilane, γ-aminopropylmethyldimethoxysilane,
N-(β-aminoethyl)-γ-aminopropyltriethoxysilane, N-(β-aminoethyl)-γ-aminopropylmethyldiethoxysilane,
dimethyldimethoxysilane, phenylmethyldimethoxysilane, dimethyldiethoxysilane, phenylmethyldiethoxysilane,
γ-chloropropylmethyldimethoxysilane, γ-chloropropylmethyldiethoxysilane, dimethyldiacetoxysilane,
γ-methacryloxypropylmethyldimethoxysilane, γ-methacryloxypropylmethyldiethoxysilane,
γ-mercaptopropylmethyldimethoxysilane, γ-mercaptopropylmethyldiethoxysilane, methylvinyldimethoxysilane,
and methylvinyldiethoxysilane.
[0033] Examples of the commercially available silane coupling agent may include the KBM-303,
KBM-402, KBM-403, KBE402, KBE403, KBM-1403, KBM-502, KBM- 503, KBE-502, KBE-503, KBM-5103,
KBM-602, KBM-603, KBM-903, KBE-903, KBE-9103, KBM-573, KBM-575, KBM-9659, KBE-585,
KBM-802, KBM-803, KBE-846, and KBE-9007 of trade names manufactured by Shin-Etsu Chemical
Co., Ltd.
[0034] The component (C) is a polyfunctional epoxy compound having two or more epoxy groups
in one molecule, and preferably it is a polyfunctional epoxy compound having two or
three epoxy groups in one molecule.
[0035] Specific examples of the component (C) may include aliphatic epoxy compounds such
as 1,6-hexanediol diglycidyl ether, ethylene glycol diglycidyl ether, diethylene glycol
diglycidyl ether, triethylene glycol diglycidyl ether, tetraethylene glycol diglycidyl
ether, nonaethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, dipropylene
glycol diglycidyl ether, tripropylene glycol diglycidyl ether, tetrapropylene glycol
diglycidyl ether, nonapropylene glycol diglycidyl ether, neopentyl glycol diglycidyl
ether, diglycidyl ether of neopentyl glycol hydroxypivalate, trimethylolpropane diglycidyl
ether, trimethylolpropane triglycidyl ether, glycerol diglycidyl ether, glycerol triglycidyl
ether, diglycerol diglycidyl ether, diglycerol triglycidyl ether, diglycerol tetraglycidyl
ether, pentaerythritol diglycidyl ether, pentaerythritol triglycidyl ether, pentaerythritol
tetraglycidyl ether, dipentaerythritol tetraglycidyl ether, sorbitol tetraglycidyl
ether, diglycidyl ether of tris(2-hydroxyethyl) isocyanurate, and triglycidyl ether
of tris(2-hydroxyethyl) isocyanurate, alicyclic epoxy compounds such as isophorone
diol diglycidyl ether and bis-2,2-hydroxycyclohexylpropane diglycidyl ether, and aromatic
epoxy compounds such as resorcinol diglycidyl ether, bisphenol A diglycidyl ether,
bisphenol F diglycidyl ether, bisphenol S diglycidyl ether, orthophthalic acid diglycidyl
ester, phenol novolac polyglycidyl ether, and cresol novolac polyglycidyl ether. As
the component (C), a compound having two or three epoxy groups (bifunctional or trifunctional
epoxy compound) is more preferable from the viewpoint of adhesive property with the
adjacent layer or the lens substrate.
[0036] Examples of the commercially available polyfunctional epoxy compound may include
the EX-201, EX-211, EX-212, EX-252, EX-313, EX-314, EX-321, EX-411, EX-421, EX-512,
EX-521, EX-611, EX-612, EX-614, and EX-614B of "DENACOL" series of a trade name manufactured
by Nagase ChemteX Corporation.
[0037] The curable composition is one that contains the components (A) to (C) described
above, and it can be prepared by mixing optional components such as an organic solvent,
a surfactant (leveling agent), and a curing catalyst with the above components if
necessary.
[0038] The content of the component (A) is preferably 20% by mass or more, more preferably
30% by mass or more, and even more preferably 40% by mass or more in the solid of
the curable composition, and it is preferably 80% by mass or less, more preferably
75% by mass or less, and even more preferably 70% by mass or less in the solid of
the curable composition.
[0039] The content of the component (B) is preferably 5% by mass or more, more preferably
10% by mass or more, and even more preferably 15% by mass or more in the solid of
the curable composition, and it is preferably 80% by mass or less, more preferably
75% by mass or less, and even more preferably 70% by mass or less in the solid of
the curable composition.
[0040] The content of the component (C) is preferably 5% by mass or more, more preferably
8% by mass or more, and even more preferably 10% by mass or more in the solid of the
curable composition, and it is preferably 40% by mass or less, more preferably 35%
by mass or less, and even more preferably 30% by mass or less in the solid of the
curable composition.
[0041] The filler/matrix ratio (hereinafter, also simply referred to as the "F/M ratio")
is preferably 0.2 or more, more preferably 0.4 or more, and even more preferably 0.7
or more, and it is preferably 2.0 or less, more preferably 1.6 or less, and even more
preferably 1.4 or less.
[0042] Incidentally, the F/M ratio means the mass ratio [component (A)/(component (B) +
component (C))] of the component (A) to the total mass of the component (B) and the
component (C).
[0043] The hard coat layer can be formed by coating a plastic lens substrate with the curable
composition and subjecting the coated curable composition to a curing treatment (heat
curing, photocuring, or the like) in accordance with the curable group. As the coating
means of the curable composition, it is possible to apply a method that is usually
used such as a dipping method, a spin coating method, a spray method. The curing treatment
is usually conducted by heating. The curing treatment by heating can be conducted,
for example, by placing a lens coated with the curable composition in an environment
having an ambient temperature of from 50 to 150°C for about 30 minutes to 3 hours.
On the other hand, the irradiation light for the curing treatment is, for example,
an electron beam or ultraviolet light. The kind of irradiation light and the irradiation
conditions are appropriately selected depending on the kind of component (C) . Generally,
it is possible to form a hard coat layer which has a high strength and contributes
to the improvement of abrasion resistance of the lens by irradiating the curable composition
with ultraviolet light at an irradiation light dose of about from 500 to 2000 mJ/cm
2.
(Primer layer)
[0044] The primer layer is, for example, an aqueous resin layer formed from an aqueous resin
composition containing a resin component and an aqueous solvent.
[0045] The aqueous solvent contained in the aqueous resin composition is, for example, water
or a mixed solvent of water and a polar solvent or the like, and it is preferably
water. The solid concentration in the aqueous resin composition is preferably from
1 to 60% by mass and more preferably from 5 to 40% by mass from the viewpoint of liquid
stability and film-forming property. The aqueous resin composition can also contain
additives such as an antioxidant, a dispersant, and a plasticizer if necessary in
addition to the resin component. In addition, a commercially available aqueous resin
composition may be used by being diluted with a solvent such as water, an alcohol,
or propylene glycol monomethyl ether (PGM).
[0046] The aqueous resin composition can contain resin component in a state of being dissolved
in an aqueous solvent or a state of being dispersed as fine particles (preferably
colloidal particles). Among them, the aqueous resin composition is desirably a dispersion
in which the resin component is dispersed in an aqueous solvent (preferably water)
in the form of fine particles. Inthiscase, the particle size of the resin component
is preferably 0.3 µm or less from the viewpoint of dispersion stability of the composition.
In addition, the pH of the aqueous resin composition is preferably about from 5.5
to 9.0 at 25°C from the viewpoint of stability. The viscosity of the aqueous resin
composition is preferably from 5 to 500 mPa·s and more preferably from 10 to 50 mPa·s
at 25°C from the viewpoint of coating suitability. In addition, an aqueous resin composition
having the following film properties is preferable in consideration of physical properties
of the aqueous resin layer to be formed. The coating film obtained by coating a glass
plate with the aqueous resin composition so as to have a thickness of 1 mm and drying
this for 1 hour at 120°C has a glass transition temperature Tg of from -58°C to 7°C,
a pencil hardness of from 4B to 2H, and a tensile strength measured in conformity
to JISK 7113 of from 15 to 69 MPa.
[0047] Examples of the resin component of the aqueous resin composition may include at least
one kind selected from a polyurethane resin, an acrylic resin, or an epoxy resin,
and preferably the resin component is a polyurethane resin. The aqueous resin composition
containing a polyurethane resin, namely, an aqueous polyurethane resin composition
can be prepared, for example, by subjecting a high molecular weight polyol compound
and an organic polyisocyanate compound to a urethanization reaction in a solvent that
is inert to the reaction and exhibits great affinity for water together with a chain
extender if necessary to obtain a prepolymer, neutralizing this prepolymer, and then
dispersing the prepolymer in an aqueous solvent containing a chain extender to increase
the molecular weight. For such an aqueous polyurethane resin composition and the preparation
method thereof, it is possible to refer to, for example, paragraphs [0009] to [0013]
in
JP 3588375 B1, the paragraphs [0012] to [0021] in
JP 8-34897 A, paragraphs [0010] to [0033] in
JP 11-92653 A, and paragraphs [0010] to [0033] in
JP 11-92655 A. In addition, as the aqueous polyurethane resin composition, it is also possible
to use a commercially available waterborne urethane as it is or by diluting it with
an aqueous solvent if necessary. As the commercially available waterborne polyurethane,
for example, it is possible to use the "EVAFANOL" series manufactured by NICCA CHEMICAL
CO. , LTD. , the "SUPERFLEX" series manufactured by DKS Co., Ltd., the "ADEKA BONTIGHTER"
series manufactured by ADEKA CORPORATION, the "OLESTER" series manufactured by Mitsui
Chemicals, Inc., the "VONDIC" series and "HYDRAN" series manufactured by DIC Corporation,
the "IMPRANIL" series manufactured by Bayer AG, the "SOFLANATE" series manufactured
by Nippon Soflan the "POIZ" series manufactured by Kao Corporation, the "SANPRENE"
series manufactured by Sanyo Chemical Industries, Ltd., the "IZELAX" series manufactured
by Hodogaya Chemical CO. , LTD. , and the "NEOREZ" seriesmanufactured by Zeneca Group
PLC.
[0048] It is possible to form an aqueous resin layer as a primer layer by coating the surface
of a substrate with the aqueous resin composition and drying the aqueous resin composition.
[0049] As the coating method, a known coating method such as a dipping method or a spin
coating method can be used. The coating conditions may be appropriately set so as
to form a primer layer having a desired film thickness. Before coating, the polarizing
film surface of the surface to be coated can also be subjected to a chemical treatment
using an acid, an alkali, various kinds of organic solvents, or the like, a physical
treatment using plasma, ultraviolet light, ozone, or the like, and a detergent treatment
using various kinds of detergents. By conducting such a pretreatment, it is possible
to improve the adhesive property.
[0050] After coating with the aqueous resin composition, an aqueous resin layer can be formed
as a primer layer by drying the composition. The drying can be conducted, for example,
by placing the member on which the primer layer is formed in an atmosphere of from
room temperature to 100°C for from 5 minutes to 24 hours.
(Interference fringe suppressing layer)
[0051] It is preferable that the spectacle lens of the present invention further includes
an interference fringe suppressing layer between the lens substrate and the hard coat
layer.
[0052] The interference fringe suppressing layer preferably has an optical film thickness
of from 0. 2λ to 0. 3λ in the light having a wavelength λ of from 450 to 650 nm in
order to suppress the interference fringe.
[0053] The interference fringe suppressing layer is obtained, for example, by coating with
a dispersion containing at least inorganic oxide particles and a resin.
[0054] The inorganic oxide particles are used from the viewpoint of adjusting the refractive
index of the interference fringe suppressing layer, and examples thereof may include
particles of tungsten oxide (WO
3), zinc oxide (ZnO), silicon oxide (SiO
2), aluminum oxide (Al
2O
3), titanium oxide (TiO
2), zirconium oxide (ZrO
2), tin oxide (SnO
2), beryllium oxide (BeO), antimony oxide (Sb
2O
5), and the like, and the inorganic oxide particles may be used singly or two or more
kinds thereof may be concurrently used. In addition, it is also possible to use composite
oxide particles of two or more kinds of inorganic oxides. The particle size of the
inorganic oxide particles is preferably in a range of from 5 to 30 nm from the viewpoint
of optical properties.
[0055] Examples of the resin of the interference fringe suppressing layer may include at
least one kind selected from a polyurethane resin, an acrylic resin, or an epoxy resin,
and preferably the resin is a polyurethane resin and more preferably it is an aqueous
resin composition containing a polyurethane resin, namely, an aqueous polyurethane
resin composition. Preferred examples of the aqueous polyurethane resin composition
may include the resins exemplified in the primer layer.
[0056] The dispersion may contain an aqueous solvent. The aqueous solvent is, for example,
water or a mixed solvent of water and a polar solvent or the like, and preferably
it is water. The solid concentration in the aqueous resin composition is preferably
from 1 to 60% by mass and more preferably from 5 to 40% by mass from the viewpoint
of liquid stability and film-forming property. The aqueous resin composition can also
contain additives such as an antioxidant, a dispersant, and a plasticizer if necessary
in addition to the resin component. In addition, a commercially available aqueous
resin composition may be used by being diluted with a solvent such as water, an alcohol,
or propylene glycol monomethyl ether (PGM).
(Antireflection layer)
[0057] An antiref lection layer is provided on the hard coat layer. The antireflection layer,
for example, has a configuration in which a low refractive index layer and a high
refractive index layer are alternately disposed. The antireflection layer has preferably
from 4 to 10 layers and more preferably from 5 to 8 layers.
[0058] The refractive index of the low refractive index layer is preferably from 1.35 to
1.80 and more preferably from 1.45 to 1. 50 at a wavelength of from 500 to 550 nm.
The low refractive index layer is formed of an inorganic oxide, and preferably it
is formed of SiO
2.
[0059] The refractive index of the high refractive index layer is preferably from 1.90 to
2.60 and more preferably from 2.00 to 2.40 at a wavelength of from 500 to 550 nm.
[0060] The high refractive index layer is, for example, formed of an inorganic oxide. The
inorganic oxide used in the high refractive index layer is preferably at least one
kind of inorganic oxide selected from ZrO
2, Ta
2O
5, Y
2O
3, TiO
2, Nb
2O
5, and Al
2O
3 and more preferably ZrO
2 or Ta
2O
5.
[0061] The spectacle lens of the present invention may have a hard coat layer and other
functional layers only on the surface of the lens substrate or on the rear surface
thereof as well. The spectacle lens is preferably a plastic lens for spectacle of
which the lens substrate is a plastic.
Examples
[0062] Hereinafter, the present invention will be described in more detail with reference
to Examples, but the present invention is not limited to these Examples. Incidentally,
the evaluation of the plastic lenses obtained in Examples and Comparative Examples
were carried out as follows.
[Average film thickness of hard coat layer]
[0063] The average film thickness of the hard coat layer was measured by using a lens substrate
on which the hard coat layer was formed and a non-contact type film thickness measuring
apparatus (non-contact film thickness measuring instrument FF 8 manufactured by SystemRoad
co., Ltd.) by the optical interference method.
[Diamond scratch test]
[0064] A diamond stylus having a tip curvature radius of 50 µm was installed to a continuous
load type surface measuring machine (Type 22 manufactured by Shinto Scientific Co.,
ltd.), the spectacle lens and the diamond stylus were linearly relatively moved at
a velocity of 10 mm/sec while gradually increasing the contact load between them at
1 g/sec to form scratches. The load was determined from the position at which the
scratches started to be visually recognized under a fluorescent lamp and adopted as
the "scratch generating load", and the scratches were observed under a microscope,
and the load was determined from the position at which the surface film of the spectacle
lens started to be cut and adopted as the "film peeling off load".
[0065] Incidentally, the color of the scratches to be formed is in a state indicating white
as the surface film is cut. In this manner, scratches conspicuous even with a naked
eye are formed when the surface film is cut.
[AR adhesion]
[0066] On the basis of JIS K5600-5-6 (ISO 2409 1992), 10 x 10 pieces of grids were formed
on a plastic lens including an antireflection layer, the peel test was conducted three
times by using cellophane pressure-sensitive adhesive tape, and the remaining grids
among the 100 pieces were counted.
* Evaluation criteria
[0067]
- A number of peeled off square meshes of 0/100 to 2/100
- B number of peeled off square meshes of 3/100 to 5/100
- C number of peeled off square meshes of 6/100 or less
[Example 1]
[0068] The primer liquid was applied on the resin substrate (plastic lens, tradename: EYNOA
manufactured by HOYA CORPORATION, refractive index: 1.67) by a dipping method and
dried and solidified for 20 minutes at 100°C to form a primer layer on both surfaces
of the lens substrate, the hard coat liquid constituted by the following components
was applied thereon by a spray method and dried for 20 minutes at 100°C to solidify
the hard coat film. On the sample surface subjected to this hard coat, a silicon oxide
layer of the first ground layer (low refractive index layer) was formed by a vacuum
deposition method, and a zirconium oxide layer and a silicon oxide layer were alternately
laminated thereon as the second layer to the seventh layer, thereby forming the antireflection
layer (AR 1).
[Examples 2 to 9 and Comparative Examples 1 to 3]
[0069] The plastic lenses were obtained in the same manner as in Example 1 except that the
configurations of the primer layer, the hard coat layer, and the AR layer were as
those presented in the following tables. The plastic lenses thus obtained were evaluated,
and the results thereof are presented in the following tables. However, the hard coat
liquid was applied by a dipping method only in Comparative Example 3.
(Primer liquid)
[0070] PR1: one prepared by diluting an aqueous polyurethane resin composition (EVAFANOLHA-170manufacturedbyNICCA
CHEMICAL CO. , LTD) 6-fold with propylene glycol monomethyl ether was used.
(Component of hard coat liquid)
[Organosilicon compound]
[0071] KBM403: γ-glycidoxypropyltrimethoxysilane (trade name: KBM403 manufactured by Shin-Etsu
Chemical Co., Ltd.)
[Polyfunctional epoxy compound]
[0072] EX-321: trimethylolpropane polyglycidyl ether (number of glycidyl group functional
groups: bi- to tri-functional, trade name: EX-321 manufactured by Nagase ChemteX Corporation)
[Inorganic oxide]
[0073]
PGM-ST: SiO2 sol (trade name: PGM-STmanufacturedbyNISSAN CHEMICAL INDUSTRIES, LTD.)
MeOH silica sol: SiO2 sol (trade name: MeOH silica sol manufactured by NISSAN CHEMICAL INDUSTRIES, LTD.)
[Others]
[0074]
Leveling material: surfactant (trade name: Y7006 manufactured by Dow Corning Toray)
Aluminum-based catalyst: aluminum tris (acetylacetonate) (trade name: aluminum chelate
A (W) manufactured by Kawaken Fine Chemicals Co., Ltd.)
Diluting solvent: methanol, PGM, 4-hydroxy-4-methyl-2-pentanone (DAA), water, and
hydrogen chloride solution
(Antireflection layer)
[0075]
AR1: low refractive index material (SiO2) and high refractive index material (ZrO2)
AR2: low refractive index material (SiO2) and high refractive index material (Ta2O5)
AR3: low refractive index material (SiO2) and high refractive index material (Nb2O5)
[0076] Representation of the substrate in the table is as follows. 167: plastic lens for
spectacle, trade name: EYNOA manufactured by HOYA CORPORATION, refractive index: 1.67
[0077] [Table 1]
Table 1
Kind of hard coat liquid |
Blended amount (parts by mass) |
Mass of solid (parts by mass) |
Amount of polyfunctional epoxy compound in matrix component (% by mass) |
Inorganic oxide |
Silane coupling agent |
Polyfunctional epoxy compound |
Leveling agent |
Aluminum-based catalyst |
Inorganic oxide |
Silane coupling agent |
Polyfunctional epoxy compound |
Kind |
Amount |
Kind |
Amount |
Kind |
Amount |
HC1 |
PGM-ST+MeOH silica sol |
23+47 |
KBM403 |
23 |
EX321 |
11 |
1 |
2.8 |
21 |
16 |
11 |
40 |
HC2 |
PGM-ST+MeOH silica sol |
23+47 |
KBM403 |
30 |
EX321 |
5 |
1 |
2.0 |
21 |
21 |
5 |
20 |
HC3 |
PGM-ST+MeOH silica sol |
23+47 |
KBM403 |
26 |
EX321 |
8 |
1 |
2.0 |
21 |
19 |
8 |
30 |
HC4 |
PGM-ST+MeOH silica sol |
19+37 |
KBM403 |
56 |
EX321 |
- |
1 |
2.0 |
17 |
40 |
- |
0 |
[0078] [Table 2]
Table 2
|
Substrate |
Primer layer |
Hard coat layer |
AR layer |
Kind |
Film thickness [µm] |
Kind |
Ratio of epoxy |
Film thickness [µm] |
Kind of AR |
Example 1 |
167 |
PR1 |
1.6 |
HC1 |
40 |
20 |
AR1 |
Example 2 |
167 |
PR1 |
1.6 |
HC2 |
20 |
20 |
AR1 |
Example 3 |
167 |
PR1 |
1.6 |
HC3 |
30 |
20 |
AR1 |
Example 4 |
167 |
PR1 |
1.6 |
HC3 |
30 |
20 |
AR1 |
Example 5 |
167 |
PR1 |
1.6 |
HC3 |
30 |
20 |
AR1 |
Example 6 |
167 |
PR1 |
1.8 |
HC1 |
40 |
10 |
AR2 |
Example 7 |
167 |
PR1 |
1.8 |
HC1 |
40 |
20 |
AR2 |
Example 8 |
167 |
PR1 |
1.8 |
HC1 |
40 |
30 |
AR2 |
Example 9 |
167 |
PR1 |
1.8 |
HC1 |
40 |
40 |
AR2 |
Comparative Example 1 |
167 |
PR1 |
1.6 |
HC4 |
0 |
20 |
AR1 |
Comparative Example 2 |
167 |
PR1 |
1.8 |
HC4 |
0 |
30 |
AR2 |
Comparative Example 3 |
167 |
PR1 |
1 |
HC4 |
0 |
3 |
AR3 |
[0079] [Table 3]
Table 3
|
Spectacle lens |
DS test |
AR adhesion |
Substrate |
Hard coat layer |
Scratch generating load [gf] |
Film peeling off load [gf] |
Ratio of epoxy*1 (% by mass) |
Film thickness [µm] |
Example 1 |
167 |
40 |
20 |
120 |
296 |
A |
Example 2 |
167 |
20 |
20 |
120 |
241 |
A |
Example 3 |
167 |
30 |
20 |
120 |
298 |
A |
Example 4 |
167 |
30 |
20 |
120 |
300 |
A |
Example 5 |
167 |
30 |
20 |
120 |
263 |
A |
Example 6 |
167 |
40 |
10 |
85 |
185 |
A |
Example 7 |
167 |
40 |
20 |
100 |
265 |
A |
Example 8 |
167 |
40 |
30 |
60 |
387 |
A |
Example 9 |
167 |
40 |
40 |
60 |
450 |
A |
Comparative Example 1 |
167 |
0 |
20 |
120 |
295 |
C |
Comparative Example 2 |
167 |
0 |
30 |
100 |
390 |
C |
Comparative Example 3 |
167 |
0 |
3 |
30 |
74 |
C |
*1 Amount of polyfunctional epoxy compound in matrix component (% by mass) |
[0080] It can be seen that a high film peeling off load and excellent scratch resistance
are obtained as the film thickness of the hard coat layer is in a predetermined range
when the results for Examples are compared with those for Comparative Examples. Additionally,
it can be seen that a hard coat layer exhibiting excellent adhesive property with
a functional layer such as an antireflection layer formed thereon as the ratio of
the polyfunctional epoxy compound in the hard coat liquid is within a predetermined
range.